Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CSM MEDIUM

K-Number: K854052 · 1985-12-31

Decision Date1985-12-31
Product CodeLYX
DecisionSubstantially Equivalent

Device Summary

CSM MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Northern Scientific, Inc.. It received FDA 510(k) clearance on 1985-12-31 under 510(k) number K854052. The device is classified under product code LYX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CSM MEDIUM?

CSM MEDIUM is a medical device that received FDA 510(k) clearance on 1985-12-31. The listed applicant is Northern Scientific, Inc.. The 510(k) number is K854052.

When did CSM MEDIUM receive FDA 510(k) clearance?

CSM MEDIUM received FDA 510(k) clearance on 1985-12-31, under 510(k) number K854052.

Who is the listed applicant for CSM MEDIUM?

The FDA 510(k) record lists Northern Scientific, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CSM MEDIUM?

The FDA product code for CSM MEDIUM is LYX.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Northern Scientific, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: LYX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑